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Detection of point mutation in dystrophin gene reveals somatic and germline mosaicism in the mother of a patient with Duchenne muscular dystrophy
Author(s) -
Essen Anthonie J. van,
Mulder Inge M.,
Vlies Pieter van der,
Hout Annemarie H. van der,
Buys Charles H.C.M.,
Hofstra Robert M.W.,
Dunnen Johan T. den
Publication year - 2002
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.10056
Subject(s) - medical genetics , medicine , duchenne muscular dystrophy , genetics , biology , gene
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